ClinGen Allele Registry
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Canonical Allele Identifier:
CA11904402
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.29901430G>A
GRCh37
chr4:g.29903052G>A
Linked Data - Sequence & Population
gnomAD v2:
4:29903052 G / A
gnomAD v3:
4:29901430 G / A
gnomAD v4:
chr4-29901430-G-A
Joint Max Group AF
0.46473597 (AFR)
Genomes Max Group AF
0.46473597 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7442317
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.29901430G>A , CM000666.2:g.29901430G>A
GRCh38
NC_000004.11:g.29903052G>A , CM000666.1:g.29903052G>A
GRCh37
NC_000004.10:g.29512150G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'